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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 916031Generated: October 30, 2026

Iodine → HCID 20796135, compound

https://huagongshe.com/reaction/916031

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantDiiodomethaneHCID 6346—
Reactant4-(5-Fluoro-2-methoxyphenyl)-2-hydroxy-2-trifluoromethylpent-4-enoic acid ethyl esterHCID 20796136—
CatalystZinc copper coupleHCID 10290809—
SolventDiethyl EtherHCID 3283—
SolventEthyl AcetateHCID 8857—
ProductHCID 20796135HCID 2079613576.6%

Reaction Steps

To a solution of 620 mg (1.84 mmol) of 4-(5-fluoro-2-methoxyphenyl)-2-hydroxy-2-trifluoromethylpent-4-enoic acid ethyl ester, 475 mg zinc copper couple, and an iodine crystal in anhydrous ether in a sealed tube warmed to 55° C. was added dropwise 500 μL (6.20 mmol) of diiodomethane. The reaction was monitored by TLC in dichloromethane-hexanes (1:1) or ether-hexanes (2:8). After 18 hours, the mixture was cooled, diluted with EtOAc and filtered through diatomaceous earth. The filtrate was washed with three 10 mL portions of 1 N aqueous HCl, 10 mL of brine, three 10 mL portions of saturated aqueous sodium bicarbonate, dried over magnesium sulfate, filtered, and concentrated. The crude material was adsorbed onto silica gel and chromatographed on silica gel using ether-hexanes (0:100, then 1:99, then 2:98) to afford 494 mg (76%) of 3,3,3-trifluoro-2-[1-(5-fluoro-2-methoxyphenyl)cyclopropylmethyl]-2-hydroxypropionic acid ethyl ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07268152B2
Source datasetuspto-grants-2007_09
ORD IDord-c97e289475ce4752aab695deed24748b
Source noteuspto-grants-2007_09